Carl Zeiss Jena GmbH
FDA 510(k) & PMA Approved Devices — 1 products
Advertisement
Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K011877 | FF450 PLUS FUNDUS CAMERA AND VISUPAC DIGITAL IMAGE ARCHIVING SYSTEM, OR FF450 PLUS VISUPAC SYSTEM | HKI | 2001-09-26 | View |
No matching devices.
Advertisement